Evidence map›Paper›PMID 33425968›Full record

ArticleFrontiers in medicine2020

Case Report: Composite Angioimmunoblastic T-Cell Lymphoma and Epstein-Barr Virus-Positive B-Cell Lymphoproliferative Disorder as Other Iatrogenic Immunodeficiency-Associated Lymphoproliferative Disorders.

Seiji Kakiuchi, Kimikazu Yakushijin, Ikumi Takagi, Junpei Rikitake, Hiroaki Akiyama, Hiroyuki Matsuba, Yoshitake Hayashi, Kazuyoshi Kajimoto, Nobuko Iwata

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Seiji KakiuchiDepartment of Hematology, Yodogawa Christian Hospital, Osaka, Japan.
Kimikazu YakushijinDivision of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.
Ikumi TakagiDepartment of Hematology, Yodogawa Christian Hospital, Osaka, Japan.
Junpei RikitakeDepartment of Hematology, Yodogawa Christian Hospital, Osaka, Japan.
Hiroaki AkiyamaDepartment of Hematology, Yodogawa Christian Hospital, Osaka, Japan.
Hiroyuki MatsubaDepartment of Hematology, Yodogawa Christian Hospital, Osaka, Japan.
Yoshitake HayashiDivision of Molecular Medicine & Medical Genetics, Department of Pathology, Kobe Graduate School of Medicine, Kobe, Japan.
Kazuyoshi KajimotoDepartment of Pathology, Hyogo Cancer Center, Akashi, Japan.
Nobuko IwataDepartment of Hematology, Yodogawa Christian Hospital, Osaka, Japan.
Yodogawa Christian Hospital · JPKobe University · JPHyogo Prefectural Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunosuppressants are widely used to treat patients with rheumatoid arthritis (RA), and their adverse effects have been known to cause other iatrogenic immunodeficiency-associated lymphoproliferative disorders (OIIA-LPDs). We report a patient with RA who had been treated with methotrexate (MTX) and tacrolimus (TAC) and who developed whole body lymphadenopathy. We simultaneously confirmed angioimmunoblastic T-cell lymphoma (AITL) through a right cervical lymph node biopsy and Epstein-Barr virus-positive B-cell lymphoproliferative disorder (EBV-positive B-LPD) through a bone marrow examination. After cessation of immunosuppressant therapy, both LPDs completely disappeared. Patients with AITL are occasionally reported to develop B-cell lymphoma through reactivation of the EBV, which leads to clonal expansion in the microenvironment. Immunohistochemistry results revealed that both LPD components were positive for EBV-encoded RNA. Moreover, in this patient, the plasma EBV DNA level was found to be high; therefore, EBV infection was a probable etiology. Synchronous coexistence of AITL and B-LPD as an OIIA-LPD has rarely been reported. This case report is the first to discuss the disappearance of both LPDs on withdrawal of immunosuppressants only. AITL occasionally accompany B-LPD; however, this composite lymphoma comprised AITL and B-LPD, and OIIA-LPDs should not be overlooked.

Indexed as

angioimmunoblastic T-cell lymphoma (AITL)clonal expansioncomposite lymphomaEpstein-Barr virus reactivationmethotrexate

Identifiers

PMID33425968
PMCPMC7785868
OpenAlexW3117982286

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.